蛋白
抗体
检测试剂盒
蛋白MARKER
分子生物学
规格：
查看说明书Dnmt3b Rabbit pAb
Cat#:DPA04725应用：WB,ICC/IF
| Product Name: | Dnmt3b Rabbit pAb |
| Cat No.: | DPA04725 |
| Clonality: | Polyclonal |
| Species Reactivity: | Human, Mouse, Rat |
| Tested Applications: | WB,ICC/IF |
| Recommended Dilution: | WB: 1:1000-1:2000 ICC/IF: 1:20-1:50 |
| Size: | 30ul 50ul 100uL |
| Format: | Liquid |
| Source: | Rabbit |
| Purification Method: | Affinity Purification |
| Isotype: | IgG |
| Conjugate: | Un-conjugated |
| Storage: | Store at -20°C. Supplied in 50nM Tris-Glycine(pH 7.4), 0.15M NaCl, 40%Glycerol, 0.01% sodium azide a |
| Immunogen: | A synthetic peptide of human Dnmt3b |
| Calculated Molecular Weight: | 96 kDa |
| Observed Molecular Weight: | 96 kDa |
| GenBank Accession Number: | Q9UBC3 |
| Gene ID (NCBI): | 1789 |
| Synonyms: | ICF; ICF1; M.HsaIIIB |
| Background: | CpG methylation is an epigenetic modification that is important for embryonic development, imprinting, and X-chromosome inactivation. Studies in mice have demonstrated that DNA methylation is required for mammalian development. This gene encodes a DNA methyltransferase which is thought to function in de novo methylation, rather than maintenance methylation. The protein localizes primarily to the nucleus and its expression is developmentally regulated. Mutations in this gene cause the immunodeficiency-centromeric instability-facial anomalies (ICF) syndrome. Eight alternatively spliced transcript variants have been described. The full length sequences of variants 4 and 5 have not been determined. [provided by RefSeq, May 2011] |
| Category: | Primary Ab |
相关产品
